5,anti-Human IL22RA1 antibody and b-Actin AC15 antibody . 10 Crosstalk between IL-22 Signaling and miR-197 Forward primer with XhoI Reverse primer with NotI Mutant primer . Migration Assay Was performed using Oris Cell Migration Assay . get BCTC Microscope model: OlympusSZX16 Research Stereomicroscope. Olympus SDF PLAPO objective lenses extra-wide zoom range of 7.0x115x. Camera model: Nikon DSD-Fi1. Acquisition software: AnalySIS getIT. Image processing software: Image-J program. Effect of antago-miR-197 on KC proliferation. HaCaT cells were transfected with antago-miR-197 or scrambled control RNA. Next, BrdU incorporation assay was performed as described in figure 1b. Methylation Assay DNA was extracted using the AllPrep DNA/RNA FFPE Kit for biopsies or by Archive Pure DNA Cell/Tissue Kits for PHK. Bisulfate reactions were done with EZ DNA Methylation-Gold Kit. The sequencing was analyzed by BioEdit. Materials Recombinant Human IL-22 cytokine was purchase from. STAT3 inhibitor was purchased from form Santa Cruz biotechnology, Inc, city, state. Anago-miR-197 was purchased from Applied Biosystems). 
Effect of antago-miR-197 on KC proliferation. HaCaT cells were transfected with antago-miR-197 or scrambled control RNA. PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19674121 24 h later cells were treated or not with the indicated IL-22 concentrations. Next, BrdU incorporation assay was performed as described in figure 1b. Chromatin Immunoprecipitation Statistical analysis Statistical significance was done using the Student’s t-test. For a single comparison, a p-value,0.05 was considered significant. Methods S1 Assay. Methods S2 Migration Assay. Gastric cancer is one of the world’s most common cancers, and chemotherapy is an important strategy against gastric cancer. Because multiple chemotherapeutic drugs of different classes are used PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19674729 to treat gastric cancer, the sensitivity of anticancer drugs to gastric cancer decreases gradually, and resistance to many different drugs with different chemical structures and different mechanisms of action can occur. This type of resistance is called multidrug resistance and significantly decreases the efficiency of therapy on gastric cancer. MDR is becoming a major problem for successful cancer treatment. It has been discovered that the major reason for MDR in cancer is the overexpression of P-glycoprotein, a product of the human MDR1 gene. P-gp is an ATP-dependent efflux pump that can decrease drug accumulation in cancer cells. It is proposed that Pgp, a well-accepted biomarker of MDR, should also be considered as a molecular target in multidrug-resistant cancer. Recent studies have demonstrated that in cancer cells with MDR, the expression levels of cyclo-oxygenase-2 and an isoform of protein kinaseC are both upregulated, and their inhibition can reverse neoplastic MDR. Pseudolaric acid B, a diterpene acid isolated from the root and trunk bark of the tree Pseudolarix kaempferi Gordon, is used in traditional Chinese medicine for its wide spectrum of biological features, such as anti-fungal effects and anti-fertility effects. In addition, its anti-angiogenic effects have also been gradually recognized in recent years. Recent studies have demonstrated that PAB induces growth inhibition, cell cycle arrest and apoptosis. Moreover, PAB reverses the multidrug resistance of cancer cells. PAB suppresses the growth of the gastric neoplastic AGS cell line and induces its apoptosis. Our previous research demonstrated that PAB also has a dramatic inhibitory effect on human gastri
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